CLASS II ONGOING Device recall · Reported 1 Apr 2020 · FDA Enforcement Report
Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen recalled
Skytron, Div. The KMW Group is recalling Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, distributed in 10 states. The recall was initiated on 5 Mar 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1569-2020
- FDA event ID
- 85252
- Recalling firm
- Skytron, Div. The KMW Group, Grand Rapids, MI
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 5 Mar 2020
- FDA classified
- 25 Mar 2020
- Reported
- 1 Apr 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Patient Monitors
Timeline
| 5 Mar 2020 | Recall initiated by company | |
| 25 Mar 2020 | Classified by FDA | +20 days |
| 1 Apr 2020 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1
Where it was distributed
AZ, CO, GA, IL, MI, MN, NJ, PA, VA, VT
ArizonaColoradoGeorgiaIllinoisMichiganMinnesotaNew JerseyPennsylvaniaVirginiaVermont
Questions about this recall
Why was it recalled?
Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury.
Which lots are affected?
Serial Numbers: 1507T719-00-0-0087 1509T719-00-0-0142 1509T719-00-0-0144 1509T719-00-0-0139 1507T719-00-0-0085 1509T719-00-0-0135 1508T719-00-0-0115 1508T719-00-0-0116 1508T719-00-0-0119 1508T719-00-0-0120 1507T719-00-0-0074 1508T719-00-0-0129 1508T719-00-0-0121 1508T719-00-0-0123 1508T719-00-0-0124 1508T719-00-0-0125 1508T719-00-0-0126 1509T719-00-0-0132 1509T719-00-0-0146 1507T719-00-0-0103 1507T719-00-0-0104 1507T719-00-0-0053 1507T719-00-0-0054 1507T719-00-0-0055 1507T719-00-0-0056 1507T719-00-0-0058 1507T719-00-0-0059 1507T719-00-0-0061 1507T719-00-0-0062 1507T719-00-0-0063 1507T719-00-0-0064 1508T719-00-0-0127 1508T719-00-0-0128 1510T719-00-0-0153 1510T719-00-0-0154 1510T719-00-0-0157 1510T719-00-0-0160 1510T719-00-0-0166 1508T719-00-0-0118 1510T719-00-0-0159 1508T719-00-0-0114 1508T719-00-0-0117 1508T719-00-0-0122
Where was it sold?
AZ, CO, GA, IL, MI, MN, NJ, PA, VA, VT
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Skytron, Div. The KMW Group
All 9| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | GCX Channel Mounting Accessory recalled by Skytron, Div. The KMW Group | Skytron, Div. The KMW Group | Other | Nationwide |
| Device | CLASS II | Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 recalled | Skytron, Div. The KMW Group | Device Malfunction | Nationwide |
| Device | CLASS II | SkyVision SDS System - Video Integration recalled | Skytron, Div. The KMW Group | Device Malfunction | Nationwide |
| Device | CLASS II | Vgdf-sky (R4-010-06) Vga TO Fiber Converter-Single Format recalled | Skytron, Div. The KMW Group | Device Malfunction | 5 states |
| Device | CLASS II | Skytron Integrity 270 Steam Sterilizer recalled | Skytron, Div. The KMW Group | Sterility | Nationwide |
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| Device | CLASS I | Bravo CF capsule delivery device, Product Number FGS recalled | Given Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | IQecg Digital ECG recalled by Midmark | Midmark | Labeling Errors | Nationwide |